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719597005: 19p13.12 microdeletion syndrome (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2017. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3317083016 19p13.12 microdeletion syndrome (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module
3317084010 19p13.12 microdeletion syndrome en Synonym Active Only initial character case insensitive SNOMED CT core module
3317085011 Monosomy 19p13.12 en Synonym Active Only initial character case insensitive SNOMED CT core module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
19p13.12 microdeletion syndrome Is a Anomaly of chromosome pair 19 false Inferred relationship Existential restriction modifier
19p13.12 microdeletion syndrome Is a Deletion of part of autosome false Inferred relationship Existential restriction modifier
19p13.12 microdeletion syndrome Associated morphology Partial monosomy true Inferred relationship Existential restriction modifier 2
19p13.12 microdeletion syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 2
19p13.12 microdeletion syndrome Finding site Chromosome pair 19 true Inferred relationship Existential restriction modifier 2
19p13.12 microdeletion syndrome Associated morphology Deletion of short arm false Inferred relationship Existential restriction modifier 3
19p13.12 microdeletion syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 3
19p13.12 microdeletion syndrome Finding site Chromosome pair 19 false Inferred relationship Existential restriction modifier 3
19p13.12 microdeletion syndrome Is a Deletion of part of chromosome 19 false Inferred relationship Existential restriction modifier
19p13.12 microdeletion syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
19p13.12 microdeletion syndrome Is a Deletion of short arm of chromosome 19 true Inferred relationship Existential restriction modifier
19p13.12 microdeletion syndrome Associated morphology Deletion of short arm true Inferred relationship Existential restriction modifier 1
19p13.12 microdeletion syndrome Finding site Short arm of chromosome false Inferred relationship Existential restriction modifier 1
19p13.12 microdeletion syndrome Finding site Chromosome pair 19 true Inferred relationship Existential restriction modifier 1
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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